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脑灌注不足、轻度认知障碍和痴呆的危险因素。

Risk factors for cerebral hypoperfusion, mild cognitive impairment, and dementia.

作者信息

Meyer J S, Rauch G, Rauch R A, Haque A

机构信息

Cerebral Blood Flow Laboratory, Veterans Administration Medical Center, 77030, Houston, TX, USA.

出版信息

Neurobiol Aging. 2000 Mar-Apr;21(2):161-9. doi: 10.1016/s0197-4580(00)00136-6.

Abstract

Putative risk factors accelerating mild cognitive decline and dementia were correlated with repeated measures of cerebral atrophy, CT, densitometry, perfusions, and cognitive testing among neurologically and cognitively normative aging volunteers. A total of 224 normative subjects at increased risk for cognitive decline were admitted to the study. Mean entry age was 59.5 +/- 15.8 years. Mean follow-up is 5.8 +/- 3.3 years. At follow-up, 22 developed mild cognitive impairment (41 CCSE >/= -3), 19 became demented-8 with Vascular type (VAD), 11 with Alzheimer's type (DAT)-and 183 remain cognitively unchanged. Cerebral atrophy, tissue densities, and perfusions were measured by Xe-CT. After age 60, cerebral atrophy, ventricular enlargement, and polio- and leuko-araiosis geometrically increased as perfusions declined. Risk factors accelerating perfusional decline, cerebral atrophy, polio-araiosis, and leuko-araiosis were: transient ischemic attacks (TIAs), hypertension, smoking, hyperlipidemia, and male gender. At age 71.5 +/- 11.9, mild cognitive impairment began accelerated by TIAs, hypertension and heart disease. Leuko-araiosis began before cognitive decline. TIAs, hypertension, and hyperlipidemia correlated with VAD. Excessive cortical perfusional decrease, gray and white matter hypodensities, and cerebral atrophy correlate with cognitive decline.

摘要

在神经和认知功能正常的老年志愿者中,加速轻度认知衰退和痴呆的假定风险因素与脑萎缩、CT、骨密度测定、灌注以及认知测试的重复测量结果相关。共有224名认知衰退风险增加的正常受试者被纳入该研究。平均入组年龄为59.5±15.8岁。平均随访时间为5.8±3.3年。随访时,22人出现轻度认知障碍(41人CCSE≥-3),19人患痴呆症——8人患血管性痴呆(VAD),11人患阿尔茨海默病型痴呆(DAT)——183人认知状态未变。通过氙CT测量脑萎缩、组织密度和灌注。60岁以后,随着灌注下降,脑萎缩、脑室扩大以及脑软化和白质疏松呈几何级数增加。加速灌注下降、脑萎缩、脑软化和白质疏松的风险因素有:短暂性脑缺血发作(TIA)、高血压、吸烟、高脂血症和男性。在71.5±11.9岁时,轻度认知障碍开始由TIA、高血压和心脏病加速。白质疏松在认知衰退之前就已出现。TIA、高血压和高脂血症与血管性痴呆相关。皮质灌注过度下降、灰质和白质密度减低以及脑萎缩与认知衰退相关。

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